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Feasibility Trial of Family-Centered Therapeutic Dance for Children With Disabilities

Study acronym: DanceDiversity
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint removed 2 → 1 primary endpoints
See other at-risk trials from University of Valencia

Record History

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  1. Notable Primary endpoint(s) modified Show 7 more changesShow less
    • Start date: Sep 15, 2025 to Oct 26, 2026
    • Enrollment increased: 30 → 36 participants
    • Primary and study completion dates: Jul 1, 2027 to Jul 2027
    • Secondary endpoints: details revised at 1 of 5 entries
    • Study description expanded, about 84 words
    • Eligibility criteria expanded, about 4 words
    • Study title shortened, about 4 words
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary aim of this exploratory cluster-randomized trial is to assess the feasibility and acceptability of delivering a school-based group therapeutic dance program through a family-centered approach for children with disabilities and to generate preliminary estimates of intervention effects and outcome variability to inform the design of a future definitive cluster-randomized controlled trial. No confirmatory effectiveness hypothesis is prespecified for this exploratory trial. Instead, the study will estimate the direction, magnitude, and precision of pre-liminary between-group differences in the primary and secondary clinical outcomes and will characterize feasibility and implementation parameters relevant to a future definitive trial.
Trial Details
NCT Number NCT07166055
Lead Sponsor University of Valencia
Conditions
(from sponsor)
Children With Disabilities
Related terms Nervous System Diseases
Enrollment 36 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov